Canonical Allele Identifier: PA2830122761
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala52Val
CA367403352
NM_033508.3:c.155C>T